Associate Clinical Project Management Director, IQB Immuno-Oncology and Cell and Gene Therapy (Spain)

apartmentIQVIA placeBarcelona calendar_month 

Experteer Overview

As Associate Clinical Project Management Director, you will lead and oversee studies to ensure timely, high-quality delivery within contracts. You’ll work with cross-functional teams to implement study strategies, manage risks, and drive financial performance.

You will own relationships with key customers and guide the team to achieve milestones across multi-country studies. This role offers impact in shaping immuno-oncology and cell/gene therapy programs at IQVIA, with a hybrid work setup and strong emphasis on leadership and collaboration.

Compensaciones / Beneficios
  • Lead bid defense preparations and presentations with Business Development for large, multi-country studies
  • Develop or support integrated study management plans with the core project team
  • Oversee strategic delivery of clinical studies, optimizing speed, quality, and cost
  • Serve as primary project liaison with customers and coordinate with IQVIA BD as needed
  • Set objectives for the project team, monitor performance, and provide leadership feedback
  • Collaborate with functional groups to achieve milestones and manage issues
  • Monitor progress, communicate proactively to stakeholders, and manage risks and contingencies
  • Coach and mentor junior team members to ensure global alignment and development
  • Ensure study quality, manage quality risks, and implement CAPAs as needed
  • Participate in executive committees as part of program leadership
  • Ensure financial success through resource management, forecasting, and profitability
  • Forecast opportunities, accelerate activities, and manage scope changes with customer agreement
  • Capture lessons learned and promote continuous improvement
  • Support corporate initiatives and act as a change advocate
  • Provide input on team members’ performance and support staff development
Responsabilidades
  • Bachelor’s degree in life sciences or related field with advanced knowledge of role
  • 10+ years of clinical research experience, including 6+ years in project management
  • Knowledge of clinical trials, regulatory requirements (ICH GCP, local laws) and protocol understanding
  • Strong communication, presentation, negotiation, and customer management skills
  • Problem solving, leadership, and organizational planning capabilities
  • Ability to manage priorities, strategic thinking, and cross-functional collaboration
  • Attention to quality, learning agility, and up-to-date knowledge
  • Proficiency with MS Office (Word, Excel, PowerPoint) and IT literacy
  • Experience in managing project finances, contracts, and change control
  • Ability to work across geographies and understand cultural differences
Requisitos principales
  • Hybrid work model
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